FDA Inspection 1005999 — Harold Boyd

Harold Boyd — FEI 3013203971

The FDA completed an inspection of Harold Boyd on Mar 14, 2017 in Fleming Island, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 14, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Fleming Island, FL (United States)

Additional Details

Clinical Investigator (CI)